52230-11-2|Lemmatoxin C|Lemmatoxin C|-范德生物科技公司

Lemmatoxin C

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names：
Lemmatoxin C
CAS号：
52230-11-2
MDL Number：
MF(分子式)： C48H78O17 MW(分子量)： 927.13
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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询价

中文别名	(6aS)-10-(((2R,3R,4S,5S,6R)-3-(((2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylic acid
英文别名	Lemmatoxin C;
CAS号	52230-11-2
SMILES	C[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](CO)O[C@@H]2O[C@@H]3[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]3OC4CCC5(C)C(CCC6(C)C5CC=C7[C@@]6(C)CCC8(C(O)=O)C7CC(C)(C)CC8)C4(C)C)O1
Inchi	InChI=1S/C48H78O17/c1-22-30(51)33(54)36(57)39(60-22)64-38-35(56)32(53)26(21-50)62-41(38)65-37-34(55)31(52)25(20-49)61-40(37)63-29-12-13-45(6)27(44(29,4)5)11-14-47(8)28(45)10-9-23-24-19-43(2,3)15-17-48(24,42(58)59)18-16-46(23,47)7/h9,22,24-41,49-57H,10-21H2,1-8H3,(H,58,59)/t22-,24?,25+,26-,27?,28?,29?,30-,31+,32-,33+,34-,35+,36+,37+,38-,39-,40-,41+,45?,46+,47?,48?/m0/s1
InchiKey	QMJCVEOVVBBZDW-XGJOVNJQSA-N
分子式 Formula	C48H78O17
分子量 Molecular Weight	927.13
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Lemmatoxin C(CAS:52230-11-2):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Lemmatoxin C is a bioactive chemical.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

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[2]Basso AV, Nicotra VE, Parra A, Martínez A, Fernández-Vivas A. Biotransformation of Salpichrolides A, C, and G by Three Filamentous Fungi. J Nat Prod. 2016 Jun 24;79(6):1658-67. doi: 10.1021/acs.jnatprod.6b00310. Epub 2016 Jun 10. PubMed PMID: 27285201.

[3] Yamada M, Tanabe Y, Dang JS, Sato S, Mizorogi N, Hachiya M, Suzuki M, Abe T, Kurihara H, Maeda Y, Zhao X, Lian Y, Nagase S, Akasaka T. D(2d)(23)-C(84) versus Sc(2)C(2)@D(2d)(23)-C(84): Impact of Endohedral Sc(2)C(2) Doping on Chemical Reactivity in the Photolysis of Diazirine. J Am Chem Soc. 2016 Dec 21;138(50):16523-16532. doi: 10.1021/jacs.6b10751. Epub 2016 Dec 7. PubMed PMID: 27998084.

[4] Filho LC, Packer L. Revision of the Neotropical subgenera Coelioxys (Platycoelioxys) Mitchell and C. (Rhinocoelioxys) Mitchell (Hymenoptera; Megachilidae) with the description of one new species. Zootaxa. 2015 Mar 31;3941(2):151-203. doi: 10.11646/zootaxa.3941.2.1. PubMed PMID: 25947503.

[5] Bai Y, Li S, Zong YN, Li XL, Zhao ZH, Kong XD. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy]. Zhonghua Yi Xue Za Zhi. 2016 Apr 26;96(16):1261-9. doi: 10.3760/cma.j.issn.0376-2491.2016.16.008. Chinese. PubMed PMID: 27122458.

6: Zhang H, Timmermann BN. Withanolide Structural Revisions by (13)C NMR Spectroscopic Analysis Inclusive of the γ-Gauche Effect. J Nat Prod. 2016 Apr 22;79(4):732-42. doi: 10.1021/acs.jnatprod.5b00648. Epub 2016 Feb 19. PubMed PMID: 26894655.7: Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations. Hemoglobin. 2016;40(2):75-84. doi: 10.3109/03630269.2015.1113990. Epub 2015 Dec 4. Review. PubMed PMID: 26635043.8: Ding L, Ishida N, Murakami M, Morokuma K. sp3-sp2 vs sp3-sp3 C-C site selectivity in Rh-catalyzed ring opening of benzocyclobutenol: a DFT study. J Am Chem Soc. 2014 Jan 8;136(1):169-78. doi: 10.1021/ja407422q. Epub 2013 Dec 16. PubMed PMID: 24341735.9: Pavuluri CM, Kawamura K. Enrichment of (13)C in diacids and related compounds during photochemical processing of aqueous aerosols: New proxy for organic aerosols aging. Sci Rep. 2016 Nov 4;

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